Multifunctional medical device

ABSTRACT

A multifunctional medical device, apparatus or system that is capable of perforating a surgical procedure or operation and also capable of attracting, collecting, removing or reducing debris generated by the surgical procedure or operation, on a subject. The apparatus comprising a plurality of electrodes, two of which are configured to be in electrical communication with or being electrically connectable to opposite poles of a source of high voltage dc electricity to ionize, attract, collect, and remove or reduce debris. At least one of the electrodes is also configured to be part of a RF circuit to perform a surgical procedure or operation such as tissue cutting, cauterization tissue sealing or coagulating at a surgical site on the subject.

FIELD

The embodiments of this disclosure relate generally to a multifunctional medical device, apparatus, or system that provides the capability to medical personnel to accomplish multiple surgical procedures or operations in a single instrument. More particularly, the embodiments of this disclosure relate to a medical device that is capable of performing a surgical procedure or operation on a subject, and also capable of reducing or removing particles generated during or following the surgical procedure or operation. Even more particularly, the embodiments of this disclosure relate to a multifunctional surgical smoke extractor for the attraction, collection, reduction, and/or removal of debris generated during or following a procedure such as a laparoscopic or other intracorporeal procedures, extracorporeal, or open surgery on a subject. The present disclosure also relates to methods of employing such a multifunctional medical device, apparatus or system or extractor to reduce or remove debris generated during or following a surgical procedure or operation on a subject.

BACKGROUND

Debris such as smoke particles, smoke, cell particles, virus, virus particles, steam are often generated during surgical procedures. Debris generated in this way obscure the view of a surgeon performing the procedure, and may also be hazardous to the health of the surgical staff. Development of smoke removal methods for conventional surgery has concentrated on removing the smoke by means of a vacuum and then venting the smoke externally of the operating theatre and/or filtering out the debris. When laparoscopic procedures are carried out, gas is introduced into the patient via access ports to inflate an area of interest of the patient's body. Smoke generated in the insufflated area, for example when diathermic or electrocautery cutting is undertaken, is sucked out and may then be filtered. The debris should be filtered out but often, in practice, they are not. Filters for such vacuum smoke removal are expensive. Often the smoke is left to permeate into the operating theatre in many procedures, causing undesirable health conditions.

Even when cryosurgery is employed, frozen vapor, droplets, or matter can be generated like fog, which is suspended in the local atmosphere. The fog too can obscure the surgeon's view and therefore may be hazardous.

US patent application publication US 2012/0,067,212 describes a surgical version of an electrostatic smoke precipitation system where an ionization wand is placed into a laparoscopic environment with an attempt to ionize the particles created by energy devices. The disclosed ionization wand is provided with a high voltage negative charge that is passed to the particles. The ionized particles are then attracted to the patient abdominal wall, via a positively charged grounding pad attached to the patient in the same way as a monopolar pad is used in monopolar electrosurgery.

US patent application publication US 2014/0,228,836 discloses an apparatus and method for removing or reducing the number of particles in an enclosed atmosphere during intracorporeal procedures. The disclosed apparatus comprises a housing adapted to be placed against the body on which a procedure is to be formed, a first electrode external to the housing for contacting the body, an elongated electrically insulated probe extending from the housing and being insertable into an intracorporeal body cavity in which a procedure is to be performed, a second electrode at the free end of the probe, and circuit means for generating voltage between said first and second electrodes. The disclosed method comprises applying a voltage between the electrodes sufficient to cause local ionization of particles within the body cavity such that they migrate away from the second electrode, thereby removing or reducing the number of particles generated during the procedure from the enclosed atmosphere at or around the site of the procedure.

SUMMARY

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode and a second electrode wherein the first electrode and the second electrode am configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage de electricity to form a dc circuit to ionize, attract, collect, remove, and/or reduce debris generated at a surgical site on a subject, and wherein the first or the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the device further comprises means to control and/or monitor the dc circuit. In an embodiment, the device further comprises means to control and/or monitor the RF circuit. In an embodiment, one of the electrodes may be configured to be used both as an ionizing electrode in the de circuit and as a cutting electrode in the RF circuit as well. In an embodiment, one of the electrodes may also be configured as a RF current return pad in the RF circuit. In an embodiment, the device may further comprise a RF current return pad in the RF circuit.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage dc electricity; a first electrode; and a second electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage de electricity to form a de circuit to ionize, attract, collect, reduce, and/or remove debris generated at a surgical site on a subject, and wherein the first or the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the device or system further comprises means to control and/or monitor the d circuit. In an embodiment, the device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the second electrode may be configured to be used as an ionizing electrode in the dc circuit and as a tissue cutting blade in the RF circuit as well.

In an embodiment, the device or system may further comprise a RF circuit current return pad. In an embodiment, the first electrode or the second electrode may be configured to be used as a RF current return pad in the RF circuit and also as a smoke particle collecting patch in the de circuit. In an embodiment where the RF current return pad is used as a smoke particle collecting patch in the dc circuit, the second electrode may then be configured to be used as an ionizing electrode in the de circuit. In an embodiment, the de circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current to prevent any hazard or damage to the subject under the surgical procedure or operation. In an embodiment, the first electrode may be configured to be used as a monopolar cutting blade in the RF circuit. In an embodiment, the medical device or system may further comprise a source of surgical radio frequency energy.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode; a second electrode; and a third electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage de electricity to form a do circuit to ionize, attract, collect, remove, and/or reduce debris generated at a surgical site on a subject, and wherein the third electrode is configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the device further comprises means to control and/or monitor the dc circuit. In an embodiment, the device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the second electrode may also be configured to be in communication with the third electrode in the RF circuit. In an embodiment, the device may further comprise a RF current return pad.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage do electricity; a first electrode; a second electrode, and a third electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage de electricity to form a dc circuit to ionize, and remove or reduce debris generated at a surgical site on a subject, and wherein the first electrode or the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy and the third electrode to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the device or system further comprises means to control and/or monitor the de circuit. In an embodiment, the device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the surgical procedure or operation is tissue sealing or tissue coagulation. In an embodiment, the dc circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current to prevent any hazard or damage to the subject under the surgical procedure or operation. In an embodiment, the second electrode may be configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy and the third electrode to form a RF circuit to perform tissue sealing or coagulation at a surgical site. In an embodiment, the medical device or system further comprises a source of surgical radio frequency energy.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode; a second electrode; a third electrode; and a fourth electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with opposite poles of a source of high voltage dc electricity to ionize, and remove or reduce debris generated at a surgical site on a subject, and wherein the third electrode and the fourth electrode are configured to be in communication with a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the device further comprises means to control and/or monitor the de circuit. In an embodiment, the device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the first electrode may also be configured to be in communication with the RF circuit.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage de electricity, a first electrode; a second electrode; a third electrode; and a fourth electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage de electricity to ionize, attract, collect, reduce, and/or remove debris generated at a surgical site on a subject; and wherein the third electrode and the fourth electrode are configured to be in communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on the subject. In an embodiment, the medical device or system further comprises means to control and/or monitor the de circuit. In an embodiment, the medical device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the first electrode or the second electrode is also configured to be in communication with or electrically connectable to the third electrode or the fourth electrode to form a RF circuit to perform tissue cutting. In an embodiment, the third electrode and the fourth electrode are configured to form a RF circuit to seal or coagulate tissues. In an embodiment, the de circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current to prevent any hazard or damage to the subject under the surgical procedure or operation. In an embodiment, the medical system may further comprise a source of surgical radio frequency energy.

In one or more of the embodiments disclosed herein, the source of high voltage de electricity may be from a main power supply through a transformer and associated de rectifier. It may also be generated remotely or may be from an outside electricity source. It may also be from a battery pack. In an embodiment, the battery pack may be attachable, detachable, removable, or separable from the device, a hand piece of the device, or the system. In an embodiment, the battery pack may be housed within the device. In an embodiment, the battery pack may be rechargeable. In an embodiment where the source of high voltage de electricity is from a rechargeable battery pack, it may be recharged directly through contact with electrical conductors. In another embodiment, the source of high voltage de electricity may be conveniently housed within the medical device. It may also be provided in other manners known in the art.

While this disclosure suggests that the electrode for ionizing the particles or matter is electrically connected to the negative pole of a de power source, and the electrode for collecting or attracting the ionized particles or matter is electrically connected to the positive pole of a dc power source, in some configurations it may be advantageous or desirable to reverse this electrical connection. In other words, in some embodiments or configurations, the electrode for ionizing the particles or matter may be electrically connected to the positive pole of a dc power source, and the electrode for collecting or attracting the ionized particles or matter may be electrically connected to the negative pole of a dc power source.

One or more of the devices or systems disclosed herein may include a tissue cutting blade. One or more of the tissue cutting blades may be an ultrasonic tissue cutter that may function to cut or otherwise effect tissue or an anatomical feature by utilizing ultrasonic waves, such as disclosed in US Patent Application Publication No. 2004/0097911, the disclosure of which is hereby incorporated by reference herein for all purposes. The tissue cutting blade may be a resistively heated blade. The resistively heated blade may be heated, and heat from the blade may be transferred to tissue or anatomical feature to cut or otherwise effect the tissue or anatomical feature. The tissue cutting blade may be an electrosurgical blade where an electrical current or signal is passed though the blade, and that electrical current or signal is transferred from the blade to the tissue or anatomical feature to cut or otherwise effect it. In any of these forms, the tissue cutting blade may generate smoke during tissue cutting or otherwise effecting the tissue.

The devices or systems described and/or shown in this disclosure may include one or more filters. The filters may function to arrest, stop, capture, collect, and/or prevent ionized debris or matter as they travel towards the collecting electrode before the particles come into contact with the colleting electrode. The filter may function to arrest, stop, capture, collect, and/or prevent liquid such as saline, blood, or other extracellular fluids from coming into contact with the colleting electrode. The filter may therefore function to keep the collecting electrode clean and free of particle and/or fluid deposit. Maintaining the collecting electrode clean and free of particles and/or fluid deposit may be advantageous as the efficiency, attraction strength and/or ability of collecting electrode to attract ionized particles and/or matter may be reduced when it is dirty and/or wet.

The one or more filters may be located at any location between the ionizing electrode and the collecting electrode. The one or more filters may be located closer to the collecting electrode rather than the ionizing electrode, or vice versa. The one or more filters may at least partially surround the collecting electrode. The one or more filters may be a sleeve-type component that at least partially covers the collecting electrode. The one or more filters may be removeably connected to the device, system, and/or collecting electrode so that the filter can be replaced when it becomes dirty and/or saturated with ionized particles or matter. The filter may be attached to the device, system, and/or collecting electrode, removed or separated, and then replaced on the device, system, and/or collecting electrode without destroying the filter and/or the device, system, and/or collecting electrode. The one or more filters may be single use or disposable. The one or more filters may be cleaned and reusable. The one or more filters may be a tear or strip that can be easily attached to the collecting electrode, or any portion of the device or system. The one or more filters may be attached to the collecting electrode and subsequently detached from the collecting electrode without affecting or otherwise damaging the function of the device, the system, the collecting electrode, the filter, or both.

The filter could be similar to the traditional folded paper element as seen in many air cleaning systems, for example, in car air intake filters or breathing circuits, or acicular mullite material. Preferably, the surface area of the filter is greater compared to its volume.

The filter may be adapted or configured to collect and filter particles between about 0.07 micrometers and 10 micrometers.

The filter may be electrically connected to the de power supply so that the filter is electrically charged. In this regard, the filter preferably has the same charge as the collecting electrode. However, the filter need not be electrically charged.

Filter as used herein may encompass one or more materials or agents having a suitable pore size, and may be made of a suitable hydrophilic or hydrophobic material.

Alternatively, or additionally, one or more of the devices or systems disclosed herein may include a wiper that is configured to dry, “wipe” clean, and/or remove particles, matter, and/or liquid from the collecting electrode.

Throughout this disclosure it is recited that at least one of the electrodes is electrically connected to a pole of the DC energy source for use in an electrostatic configuration and also electrically connected to a pole of the AC energy source for use in an electrosurgical configuration. It is understood that this electrode may be at common potential with the pole of the DC energy source, and also at a common potential with the pole of the AC energy source.

Throughout this disclosure it is recited that at least one of the electrodes is electrically connected to a pole of the DC energy source for use in an electrostatic configuration and also electrically connected to a pole of the AC energy source for use in an electrosurgical configuration. The pole of the DC source and the pole of the AC source may have the same potential (e.g., both are a negative pole or a positive pole), or the poles may be different (e.g., one of the poles is negative and the other pole is positive).

The AC energy source and the DC energy source may separate and discrete source that are contained in a single, common generator. One or more instrument cables may extend between the medical device and the single, common generator. For example, one or more instrument cables may extend between the medical device and the generator for connecting the electrodes thereto. One or more electrical cables may extend between the generator and any remote electrodes or remote electrode pads. The AC energy source and the DC energy source may be separate and discrete sources that are not contained in a single, common generator, but are instead separate components. One or more instrument cables may extend between the medical device and each individual energy source. One or more electrical cables may extend between each of the generators and any remote electrodes or remote electrode pads.

In one or more of the embodiments disclosed herein, the medical device or system further comprises a dc electricity controller and/or monitor to control and/or monitor the current circulating in the de circuit to be within a safe limit. In one or more of the embodiments disclosed herein, the medical device or system further comprises a RF current or voltage controller and/or monitor to control and/or monitor the current or voltage in the RF circuit to maintain the safety and/or the different functions of the RF circuit.

In an embodiment, the de circuit of the medical device or system may be configured to be operable simultaneously, concurrently, alternatively, intermittently, or sequentially with the RF circuit to ionize, attract, collect, remove, and/or reduce debris while the RF circuit is turned on to perform a surgical procedure or operation. In an embodiment, the electrical communication of the electrodes in the dc circuit and the electrical communication of the electrodes in the RF circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially. In some embodiments, the de circuit may be turned on during or after a surgical procedure or operation.

In another embodiment, the medical device may be a standalone smoke extractor comprising an elongated member having a proximal end, a distal end, an outer surface, and a lumen extending through the elongated member; a first electrode attached to the distal end of the elongated member; a second electrode disposed over the outer surface of the elongated member; and a handle or housing attached to the proximal end of the elongated member; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity. In an embodiment, the first electrode is configured to be longitudinally movable along the lumen of the elongated member. In an embodiment, the smoke extractor further comprises means to control and/or monitor the de circuit. In an embodiment, the means to control and/or monitor the d circuit is disposed in the handle. In an embodiment, the smoke extractor further comprises a source of high voltage dc electricity disposed in the handle. In an embodiment, the source of the high voltage dc electricity is in the form of a detachable battery pack positionable in the handle portion of the extractor. In an embodiment, the first electrode is configured to be the particle ionizing electrode and the second electrode is configured to be the particle collecting electrode. In an embodiment, the elongated member is configured to be tubular for easy insertion through an access port into a surgical site on a subject.

In a further embodiment, the present disclosure also provides a method of removing or reducing smoke related particles during a surgical procedure or operation on a subject, the method comprising providing a source of high voltage de electricity; providing a device or system according to any one of the above described disclosure and variations thereof, properly connecting the device or system with the source of high voltage dc electricity; properly positioning the device at a surgical site of a subject where a surgical procedure is to be performed, and properly turning on the device or the system to ionize debris towards one electrode of the device and attract the ionized debris towards the other electrode of the device to remove or reduce the debris from the surgical site of the subject.

In another embodiment, the present disclosure provides a method of removing or reducing smoke related particles during a surgical operation on a subject, the method comprising providing a source of high voltage de electricity; providing a device or a system according to any one of the above described disclosure and variations thereof wherein the device or system has two electrodes in the do circuit; properly connecting the two electrodes with the device or the system; properly positioning the two electrodes of the device into a surgical site where a surgical procedure is to be performed; and properly turning on the device or the system to ionize debris towards one electrode of the device and attract the ionized debris towards the other electrode of the device to remove or reduce the debris from the surgical site of the subject.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein one electrode is configured to perform both smoke particle ionization in the de circuit and tissue cutting in the RF circuit.

FIG. 2 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage de electricity is disposed with the electrodes in the same block, and additionally, the ionizing electrode in the dc circuit is also configured to be used as a cutting electrode in the RF circuit.

FIG. 3 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage de electricity is disposed with the electrodes in the same block, and additionally, one electrode in the dc circuit is also configured to be used as a switchable sealing electrode in the RF circuit.

FIG. 4 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage de electricity is disposed with the electrodes in the same block, and additionally, one electrode in the de circuit is also configured to be used as a non-switchable sealing electrode in the RF circuit.

FIG. 5 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage dc electricity is disposed with the electrodes in the same block, and additionally, one electrode in the de circuit is also configured to be used as a non-switchable sealing electrode in the RF circuit.

FIG. 6 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage do electricity is disposed separately from the electrodes, and additionally, one electrode in the de circuit is also configured to be used as a non-switchable sealing electrode in the RF circuit.

FIG. 7 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage do electricity is disposed separately from the electrodes, and additionally, one electrode in the de circuit is also configured to be used as the cutting electrode in the RF circuit.

FIG. 8 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage dc electricity is disposed separately from the electrodes, and additionally, the particle collecting patch in the dc circuit is also configured to be used as the ground pad electrode in the RF circuit.

FIG. 9 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage de electricity is disposed separately from the electrodes, and additionally, the particle collecting patch electrode in the de circuit is configured to be movable or external.

FIG. 10 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage do electricity is disposed separately from the electrodes, and additionally, one electrode in the dc circuit is also configured to be used as a non-switchable sealing electrode in the RF circuit.

FIG. 1I is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the de circuit and the RF circuit are independent and yet their respective electrodes are disposed in the same block.

FIG. 12 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage de electricity is disposed separately from the electrodes, and additionally, there is a capacitor between the two sealing electrodes in the RF circuit.

FIG. 13 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure wherein the source of the high voltage dc electricity is disposed separately from the electrodes, and additionally, both sealing electrodes in the RF circuit are configured to be used as one of the two electrodes in the dc circuit.

FIG. 14 is a schematic representation of a device or system in accordance with one embodiment of the present disclosure arranged in an operation for the removal or reduction of debris generated during a surgical procedure or operation at a site such as the abdomen of a subject.

FIG. 15 is a schematic representation of a device in accordance with another embodiment of the present disclosure arranged in an operation for the removal or reduction of debris generated during a surgical procedure or operation at a site such as the abdomen of a subject.

FIG. 16 is another schematic representation of a device in accordance with one embodiment of the present disclosure wherein the two electrodes of the de circuit and the two electrodes of the RF circuit are all disposed in the insertable portion of the device.

FIG. 17 is a schematic representation of a device or system that includes one or more of the electrode configurations discussed and/or illustrated herein.

FIG. 18 is a schematic representation of a device or system that includes one or more of the electrode configurations discussed and/or illustrated herein.

FIG. 19 is a schematic representation of a device or system that includes one or more of the electrode configurations discussed and/or illustrated herein.

FIG. 20 is a schematic representation of a device or system arranged in an operation for the ionization, attraction, reduction, and/or removal of debris generated during a surgical procedure or operation at a site.

FIG. 21 is a schematic representation of a device or system arranged in an operation for the ionization, attraction, reduction, and/or removal of debris generated during a surgical procedure or operation at a site.

DETAILED DESCRIPTION

This application claims priority to U.S. patent application Ser. No. 14/865,420 filed on Sep. 25, 2015, the disclosure of which is hereby incorporated by reference herein for all purposes.

The explanations and illustrations presented herein are intended to acquaint others skilled in the art with the disclosure, its principles, and its practical applications. Those skilled in the art may adapt and apply the disclosure in numerous forms, as may be best suited to the requirements of a particular use. The specific embodiments of the present disclosure as set forth are not intended to be exhaustive or limiting of the invention. The scope of the invention should be determined not with reference to the above description, but should be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.

The terms “one embodiment”, “an embodiment”, “another embodiment”, “some embodiments”, “other embodiments”, and similar expressions indicate that the embodiment or embodiments described may include a particular feature, structure, or characteristic, but every embodiment may not necessarily include the particular feature, structure, or characteristic. Moreover, such phrases are not necessarily referring to the same embodiment. Furthermore, when a particular feature, structure, or characteristic is described in connection with an embodiment, it would be within the knowledge of one skilled in the art to incorporate such feature, structure, or characteristic into other embodiments, whether or not explicitly described, unless clearly stated to the contrary. That is, the various individual elements described below, even if not explicitly shown in a particular combination, are nevertheless contemplated as being combinable with each other to form other additional embodiments or to complement and/or enrich the described embodiment or embodiments, as would be understood by one of ordinary skill in the art.

The articles “a”, “an” and “the” are used herein to refer to one or to more than one (i.e. to at least one) of the grammatical object of the article unless otherwise clearly indicated by contrast. By way of example, “an element” means one element or more than one element.

The term “including” is used herein to mean, and is used interchangeably with, the phrase “including but not limited to”. The term “or” is used herein to mean, and is used interchangeably with, the term “and/or”, unless context clearly indicates otherwise.

The term “such as” is used herein to mean, and is used interchangeably, with the phrase “such as but not limited to”. Unless specifically stated or obvious from context, as used herein, the term “about” is understood as within a range of normal acceptance in the art, for example within standard deviations of the mean.

In this specification the terms such as “particles”, “smoke”, “fog”, “smoke particles”, and related terms are intended to encompass any particles, or molecules or matter suspended in an atmosphere including suspended droplets formed by heat or cold. Debris may include smoke, cell particles, virus, virus particles, steam.

In this specification, the term “a de circuit” means that the components of the circuit are powered by a source of direct current voltage electricity. It does not mean it is a closed system. It may comprise further components in addition to those explicitly indicated ones. It is mainly used throughout the specification for the purpose of differentiating it from a RF circuit where a radio frequency energy source is used.

In this specification, the term “a RF circuit” means that the components of the circuit are powered by a source of surgical radio frequency energy or a source of alternating current (ac). It does not mean it is a closed system. It may comprise further components in addition to those explicitly indicated ones. It is mainly used throughout the specification for the purpose of differentiating it from a dc circuit where a direct current (de) electricity energy source is used.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode and a second electrode wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity to form a de circuit to attract, ionize, and remove or reduce debris generated at a surgical site on a subject, and wherein the first or the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical alternating current or radio frequency energy to form a RF circuit to perform a surgical procedure on the subject. In an embodiment, the device further comprises means to control and/or monitor the de circuit. In an embodiment, the device further comprises means to control and/or monitor the RF circuit. In an embodiment, one of the electrodes may be configured to be used both as an ionizing electrode in the dc circuit and as a cutting electrode in the RF circuit as well. In an embodiment, one of the electrodes may also be configured as a RF current return pad in the RF circuit. In an embodiment, the device may further comprise a RF current return pad in the RF circuit.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage dc electricity; a first electrode; and a second electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage dc electricity to form a de circuit to ionize, attract, collect, reduce, and/or remove debris, and wherein the first or the second electrode is also configured to be in communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation. In an embodiment, the device or system further comprises means to control and/or monitor the de circuit. In an embodiment, the device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, one of the electrodes may be configured to be used as an ionizing electrode in the de circuit and as a tissue cutting blade in the RF circuit as well. In an embodiment, the device may further comprise a RF current return pad. In an embodiment, the RF current return pad may also be configured to be used as a smoke particle attracting or collecting patch in the de circuit to remove or reduce debris from the surgical site. In an embodiment where the RF current return pad is used as a smoke particle attracting or collecting patch in the dc circuit, the first electrode is then configured to be used as an ionizing electrode in the dc circuit. In an embodiment, the dc circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current to prevent any hazard or damage to the subject under the surgical procedure or operation. In an embodiment, one of the electrodes may be configured to be used as a monopolar cutting blade in the RF circuit. In an embodiment, the medical system further comprises a source of alternating current or surgical radio frequency energy.

In an embodiment where the second electrode is configured to be used as an ionizing electrode to ionize debris, the first electrode is then configured to be used as a smoke particle attracting and collecting electrode to attract and collect the ionized debris towards the first electrode, and consequently removing or reducing debris from the surgical site. In this embodiment, the first electrode is configured to have a large surface area in order to facilitate the collection of the ionized debris. In this embodiment, both of the first and the second electrodes may be configured to be positionable at or near the surgical site. In this embodiment, the first electrode may be disposed over the second electrode with insulating material to separate the two electrodes from direct physical contacts. The insulating material may be Al₂O₃, boron nitride, porcelain, steatite, zironia, PTFE, reinforced mica, silicon rubber, or other ceramic materials such as disclosed in U.S. Pat. Nos. 3,970,088 and 6,942,662. In this embodiment, the first electrode may be made to be tubular. In this embodiment, the second electrode may be a needle or lancet type of electrode for better ionization.

It would be appreciated that methods and materials for manufacturing different types of electrodes are well known in the art, for example, as disclosed in U.S. Pat. Nos. 4,862,890, 4,958,539, 8,357,155, and 8,852,183. It should be understood that all the electrodes described throughout this disclosure may be similarly made. Consequently, no further additional descriptions of electrodes will be attempted for subsequent sections unless otherwise specifically indicated.

In an embodiment where the first electrode in the de circuit is configured to be used as a smoke particle collecting patch in the de circuit and as the RF current return pad in the RF circuit, the second electrode in the de circuit is then configured to be used as a smoke particle ionizing electrode. The second electrode may also be configured to be used as a cutting blade for cutting tissues. In this embodiment, the RF current return pad may be made separate or detachable from the site of the surgical procedure or operation. In this embodiment, the RF current return pad may be positioned away from the surgical site such as under the skin of the subject.

In an embodiment where the electrode is configured to be used as a cutting blade, debris may be produced during the cutting process. These debris may be ionized, attracted, collected, and removed or reduced by the electrodes in the dc circuit disposed in the same device. In an embodiment, the de circuit may be powered by a battery pack. In an embodiment, the battery pack may be detachable or rechargeable.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a handle member; an elongated member attached to the housing or handle member, the elongated member having a proximal end, a distal end, an outer surface, and a lumen extending through the elongated member; a first electrode disposed inside the lumen of the elongated member; and a second electrode disposed over the outer surface of the elongated member wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage de electricity to form a dc circuit to ionize, attract, collect, and to reduce or remove debris, and wherein the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation. In an embodiment, the medical device further comprises means to control and/or monitor the de circuit. In an embodiment, the medical device further comprises means to control and/or monitor the RF circuit. In an embodiment, the device may further comprise a source of high voltage de electricity detachably positioned inside the handle member. In an embodiment, the first electrode may be configured to be a smoke particle collecting electrode. In an embodiment, the first electrode may be configured to cover most of the surface area of the elongated member. In an embodiment, the second electrode may be made to be movable along the elongated member. In an embodiment, the device may be capable of performing tissue cutting. In an embodiment, the device may be capable of performing monopolar or bipolar tissue cutting. In an embodiment where the second electrode is configured to be used in the de circuit to ionize debris, it may also be configured to be used as a cutting blade in the RF circuit to perform tissue cutting. In an embodiment, the device may further comprise a RF current return pad external to the handle.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode; a second electrode; and a third electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity to form a dc circuit to ionize, attract, collect, and remove or reduce debris generated at a surgical site on a subject, and wherein the third electrode is configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure on the subject. In an embodiment, the medical device further comprises means to control and/or monitor the dc circuit. In an embodiment, the medical device further comprises means to control and/or monitor the RF circuit. In an embodiment, the first electrode may also be configured to be in communication with the third electrode in the RF circuit. In an embodiment, the device may further comprise a RF current return pad.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage dc electricity; a first electrode; a second electrode; and a third electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage dc electricity to form a dc circuit to ionize, attract, collect, and remove or reduce debris generated at a surgical site on a subject, and wherein the first electrode or the second electrode is also configured to be in electrical communication with or electrically connectable to a source of surgical radio frequency energy and the third electrode to form a RF circuit to perform a surgical procedure or operation.

In an above embodiment, the second electrode may be configured to be used as an ionizing electrode in the dc circuit and also as a sealing electrode in the RF circuit. In an embodiment where the second electrode is configured to be used as both an ionizing electrode in the dc circuit and also as a sealing electrode in the RF circuit, the first electrode may be configured to be used as a smoke particle collecting electrode to attract and collect the ionized debris towards the first electrode, thereby attracting removing or reducing the debris from the surgical site. In this embodiment, the first electrode may be made to possess a large surface area. In this embodiment, the first electrode may be disposed over the second electrode through insulating material. In this embodiment, the first electrode may be disposed over the third electrode through insulating material. In this embodiment, the first electrode may be disposed over both the second and the third electrodes through insulating material. In an embodiment, the medical device or system may further comprise a source of surgical radio frequency energy.

In an embodiment where the second electrode is configured to be used as an ionizing electrode in the dc circuit, the first electrode and the third electrode may be configured to perform tissue sealing or coagulation in the RF circuit. In an embodiment where the second electrode is configured to be used as an ionizing electrode in the dc circuit, the second electrode is then configured to be used as a smoke particle attracting and collecting patch. In an embodiment, the de circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current in the de circuit to prevent any hazard or damage to the subject under the surgical procedure or operation. In an embodiment, the second electrode may be configured to be in communication with the third electrode to form a RF circuit to perform a bipolar tissue sealing or tissue coagulation.

In an embodiment where an electrode is configured to be used both as a scaling electrode in the RF circuit and as a smoke particle collecting patch in the dc circuit, the electrode should be made to possess a large surface area to facilitate attraction and collection of ionized smoke particle and to more efficiently disperse the RF return current.

In an embodiment, the present disclosure provides a multifunctional medical system comprising a housing or handle member; an elongated member having a proximal end, a distal end, and an outer surface, the proximal end of the elongated member attached to the handle member; a first electrode attached to the distal end of the elongated member; a second electrode also attached to the distal end of the elongated member; and a third electrode disposed over the outer surface of the elongated member; wherein the second electrode and the third electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity to form a de circuit to attract, collect, ionize, and to remove or reduce debris generated at a surgical site on a subject, and wherein the first electrode and the second electrode are also configured to be in electrical communication with or electrically connectable to the source of the surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation. In an embodiment, the system may further comprise a source of high voltage dc electricity detachably disposed inside the handle member. In an embodiment, the third electrode may be configured to cover the majority of the outer surface of the elongated member. In an embodiment the elongated member may be tubular. In an embodiment, the medical system may further comprise a source of surgical radio frequency energy.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a first electrode; a second electrode; a third electrode; and a fourth electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with opposite poles of a source of high voltage dc electricity to ionize, and remove or reduce debris generated at a surgical site on a subject, and wherein the third electrode and the fourth electrode are configured to be in communication with or electrically connectable to a source of the surgical radio frequency energy to form a RF circuit to perform a surgical procedure on the subject. In an embodiment, the medical device further comprises means to control and/or monitor the dc circuit. In an embodiment, the medical device further comprises means to control and/or monitor the RF circuit. In an embodiment, the first electrode may also be configured to be in communication with the RF circuit.

In an embodiment, the present disclosure provides a multifunctional medical device or system comprising a source of high voltage dc electricity; a first electrode; a second electrode; a third electrode; and a fourth electrode; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of the source of high voltage de electricity to ionize, attract, collect, and reduce or remove debris generated at a surgical site on a subject; and wherein the third electrode and the fourth electrode are configured to be in communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation. In an embodiment, the medical device or system further comprises means to control and/or monitor the de circuit. In an embodiment, the medical device or system further comprises means to control and/or monitor the RF circuit. In an embodiment, the first electrode or the second electrode may also be configured to be in communication with or electrically connectable to the third electrode or the fourth electrode to form a RF circuit to perform tissue cutting.

In an embodiment where the second electrode is configured to be used as an ionizing electrode in the de circuit, the first electrode is configured to be used as a smoke particle attracting and collecting patch in the dc circuit. In an embodiment where the second electrode is configured to be used as an ionizing electrode in the de circuit and also as a cutting blade in the RF circuit, the second electrode may then be configured to be in communication with either the third electrode or the fourth electrode to form a bipolar cutting device. In an embodiment, the medical system may further comprise a source of surgical radio frequency energy.

In an embodiment, the present disclosure provides a multifunctional medical device comprising a handle member; an elongated member attached to the handle member, the elongated member having a proximal end, a distal end, an outer surface, and a lumen extending though the elongated member; a first electrode attached to the distal end of the elongated member; a second electrode also attached to the distal end of the elongated member; a third electrode also attached to the distal end of the elongated member; and a fourth electrode disposed over the outer surface of the elongated member; wherein the first electrode and the second electrode are configured to be in communication with or electrically connectable to a source of surgical radio frequency energy to form a RF circuit to perform a surgical procedure or operation on a subject; and wherein the third electrode and the fourth electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity to ionize, and reduce or remove debris generated at a surgical site on the subject. In an embodiment, the third electrode may also be configured to be in communication with or electrically connectable to the first electrode or the second electrode to perform a bipolar tissue cutting. In an embodiment, the third electrode may be configured to be movable along the elongated member. In an embodiment, the medical system may further comprise a source of surgical radio frequency energy.

In an embodiment, the source of high voltage dc electricity may be detachably positioned inside the handle member. In an embodiment, the fourth electrode may be made to cover the majority of the outer surface of the elongated member. In an embodiment, all the four electrodes may be disposed in front portion of the elongated member. In an embodiment, all the four electrodes may be disposed in the insertable front portion of the elongated member.

In all the above embodiments, the source of high voltage dc electricity may be from a main power supply through a transformer and associated dc rectifier. It may also be generated remotely or may be from an outside electricity source. It may also be from a battery pack. In an embodiment, the battery pack may be detachable, removable, or separable from the device. The battery pack can be attached to the device, detached from the device, and reattached to the device one or more times without destroying the functionality of the device, the battery pack, and/or any components or features thereof. In an embodiment, the battery pack may be housed within the device. In an embodiment, the battery pack may be rechargeable. In an embodiment where the source of high voltage de electricity is from a rechargeable battery pack, it may be recharged directly through contact with electrical conductors. In another embodiment, the source of high voltage dc electricity may be conveniently housed within the medical device. It may still be provided in some other manners that are within the grasp of an ordinary skilled person in the art.

In all the above embodiments, the source of high voltage de electricity is from an electrical supply within a range of about 1 kV to about 30 kV, and preferably around 5 kV to 15 kV. Although a dc voltage of up to 30 kV could be used, lower voltages will be sufficient. For example, around 8 or 9 kV is envisaged, with a current limiting regulator in the form of a series resistor maintaining the current at a safe limit for the patient and operator. A clean reasonably constant voltage is preferred, but a voltage which is fluctuating could be used, particularly where the device is employed in conjunction with an electrically driven surgical tool, provided there is no current reversal. In this description ‘dc’ is intended to cover an oscillating or a noisy voltage which is biased to provide current only in one direction in a circuit.

In all the above embodiments, the device or the system further comprises at least one dc electricity controller or monitor to control or monitor the current circulating in the dc circuit to be within a safe limit. In order to improve safety, it is envisioned that a control means will be provided to monitor the current travelling in the high voltage circuit, which will stop the flow of current very quickly should the current increase rapidly in a short space of time, i.e. should a short circuit be detected, for example where the second electrode touches the body of the patient. This will avoid or reduce accidental voltage shocks to the patient. In addition, it is possible to monitor increased impedance of the ionizing electrode, and thereby detect a blocked electron emission. It may be possible to monitor increased impedance of the collecting electrode, and thereby detect a blocked electron collection. The current regulator is capable of limiting the amount of current flowing across the high voltage de circuit to a certain amount such as less than 10 μA, for example around 5 μA.

In all the above embodiments, the device or system further comprises at least a RF current or voltage controller or monitor to control or monitor the current or voltage in the RF circuit to maintain the safety and/or efficiency of the RF circuit.

In all the above embodiments, the de circuit further comprises a RF isolation transformer for removing or eliminating any undesired RF current to prevent any hazard or damage to the subject under the surgical procedure or operation.

In all the above relevant embodiments, the means to control the dc circuit and the means to control the RF circuit can be easily and conveniently achieved through various control means such as in the form of knobs, touches, push buttons, slides, switches and other tools/devices such as disclosed, for example, in U.S. Pat. Nos. 5,312,327 and 5,472,442, and PCT application publication No. WO 2014/151560. These tools/devices may be handled by hand, or by foot. They may be handled remotely or automatically. The means may also be in the form of a computer or some computerized tools with the ability to control and/or monitor current or voltage both in a de circuit and in a RF circuit.

It's to be understood throughout this disclosure that conductor or wiring lines connecting different components in the de circuit and in the RF circuit are all insulated from each other. These lines may be isolated (e.g. each may extend from one component to another component without commonality with other lines). These lines may be joined together to minimize the lines and complexity of these cable lines necessary for connectivity. The design and construction of this type of conductor or wiring lines are well within the grasp of a skilled person in the art.

In all the above embodiments, the source of surgical radio frequency energy should have a frequency of between 100 KHz and 100 MHz for tissue cutting, tissue sealing or coagulation, or tissue cauterization. More preferable, the frequency should be between 300 kHz and 2 MHz. Different surgical RF generators are known in the art for both monopolar and bipolar purposes. These surgical RF generators are well known in the art for purposes of tissue separation or cutting, tissue coagulation or sealing, or tissue cauterization.

In an embodiment, the de circuit of a device or system in accordance with any one of the above described or variations thereof may be configured to be operable to attract, collect, remove or reduce debris simultaneously, concurrently, alternatively, intermittently, or sequentially while the RF circuit of the device is also in operation to perform a surgical procedure or operation. In some embodiments, the de circuit of the device or system may be turned on during or after the surgical procedure or operation.

In another embodiment, the medical device may be a standalone smoke or particle extractor comprising an elongated member having a proximal end, a distal end, an outer surface, and a lumen extending through the elongated member; a first electrode attached to the distal end of the elongated member; a second electrode disposed over the outer surface of the elongated member; and a handle attached to the proximal end of the elongated member; wherein the first electrode and the second electrode are configured to be in electrical communication with or electrically connectable to opposite poles of a source of high voltage dc electricity. In an embodiment, the first electrode is configured to be longitudinally movable along the lumen of the elongated member. In an embodiment, the smoke extractor further comprises means to control and/or monitor the dc circuit. In an embodiment, the means to control and/or monitor the dc circuit is disposed in the handle. In an embodiment, the smoke extractor further comprises a source of high voltage dc electricity disposed in the handle. In an embodiment, the source of the high voltage de electricity is in the form of a detachable battery pack positionable in the handle portion of the extractor. The battery pack may be detachable from the medical device or the handle of the medical device. In an embodiment, one of the two electrodes is configured to be the particle ionizing electrode and the other of the two electrodes is configured to be the particle attracting and collecting electrode. In an embodiment, the elongated member is configured to be tubular for easy insertion through an access port into a surgical site on a subject.

In the above embodiments, the device or system may further include an introducer tool such as an endoscope, a catheter, an access sheath, or an access port.

In a further embodiment, the present disclosure also provides a method of removing or reducing smoke related particles during a surgical procedure or operation on a subject, the method comprising providing a source of high voltage dc electricity; providing a device or system according to any one of the above described disclosure and variations thereof, properly connecting the device or system with the source of high voltage dc electricity; properly positioning the device at a surgical site of a subject where a surgical procedure is to be performed, and properly turning on the device or the system to ionize debris with one electrode of the device and attract the ionized debris towards the other electrode of the device to collect, remove or reduce the debris from the surgical site of the subject.

In another embodiment, the present disclosure provides a method of removing or reducing debris or smoke related particles during a surgical operation on a subject, the method comprising providing a source of high voltage de electricity; providing a device or a system according to any one of the above described disclosure and variations thereof wherein the device or system has two electrodes in the dc circuit; properly connecting the two electrodes with the device or the system; properly positioning the two electrodes of the device into a surgical site where a surgical procedure is to be performed; and properly turning on the device or the system to ionize debris towards one electrode of the device and attracting the ionized debris towards the other electrode of the device to collect, remove or reduce the debris from the surgical site of the subject.

In another embodiment, the present disclosure provides a method of removing or reducing smoke related particles during a surgical operation on a subject, the method comprising providing a source of high voltage de electricity; providing a source of surgical RF energy; providing a device or a system according to any one of the above described disclosure and variations thereof wherein the device or system has two electrodes in the dc circuit and two electrodes in the RF circuit; properly connecting the two dc electrodes of the device or the system with the source of high voltage dc electricity; properly connecting the two RF electrodes of the device or system with the source of surgical RF energy; properly positioning the device into a surgical site where a surgical procedure is to be performed; and properly actuating the RF circuit of the device or the system to perform a surgical procedure or operation wherein debris are generated; and properly actuating the dc circuit of the device or system to ionize the generated debris towards one dc electrode of the device and attract the ionized debris towards the other de electrode of the device or system to collect, remove or reduce the debris from the surgical site of the subject. In an embodiment, the surgical procedure or operation is performed with smoke particle reduction or removal simultaneously, concurrently, alternatively, intermittently, or sequentially.

In an embodiment, the de source is removable or detachable from the device or hand piece without destroying the de source and the device or hand piece. In this regard, the device includes a detachable and/or separable lead between the de source and the ionizing electrode that permits such detachment and attachment without destroying the electrode, the lead, the device, the hand piece, or a combination thereof.

It will be apparent to the skilled addressee that many modifications, variants and improvements are possible within the ambit of the invention defined herein. For example, a device in accordance with some embodiments as described may be employed during the extracorporeal procedure.

The medical device may include a first electrode and a second electrode. The medical device may be operable in an electrostatic configuration. In the electrostatic configuration, the first electrode may be in electrical communication with a first pole of a DC energy source and the second electrode is in electrical communication with a second pole of the DC energy source. In this electrostatic configuration, the first electrode and the second electrode are configured to cooperate to ionize and attract debris from a surgical site when the medical device is operated in the electrostatic configuration. In this electrostatic configuration, the DC energy source, the first electrode, and the second electrode cooperate to complete a monopolar electrical circuit. In this electrostatic configuration, the first electrode or the second electrode may be a remote electrode pad. In this electrostatic configuration, the DC energy source, the first electrode, and the second electrode cooperate to complete a bipolar electrical circuit. In the electrosurgical configuration, the first electrode is in electrical communication with a first pole of an AC energy source and the second electrode is in communication with a second pole of the AC energy source. The first electrode and the second electrode are configured for use in an electrosurgical procedure at the surgical site when the medical device is operated in the electrosurgical configuration. In this electrosurgical configuration, the DC energy source, the first electrode, and the second electrode cooperate to complete a monopolar electrical circuit. In this electrosurgical configuration, the first electrode or the second electrode is a remote electrode pad. In this electrosurgical configuration, the DC energy source, the first electrode, and the second electrode cooperate to complete a bipolar electrical circuit. In this electrosurgical configuration, the first electrode and the second electrode are arms of a forceps device. The AC energy source and the DC energy source may be located in the same generator, or the sources may be separate and discrete sources. The DC energy source may be located in the handle or hand piece of the medical instrument, and may be attachable, detachable, and attachable one or more time without destroying the structure or function of the medical instrument, the DC energy source, or both. The DC energy source may be rechargeable. The DC energy source may be rechargeable via the AC energy source. The instrument may operate in the electrosurgical configuration before operating in the electrostatic configuration so that the instrument can attract or collect debris created while the instrument is operating in the electrosurgical configuration. The instrument may also be operable in a simultaneous electrosurgical configuration and electrostatic configuration.

The principles of the present disclosure may be better understood with reference to the drawings and the accompanying descriptions, wherein like reference numerals have been used throughout to designate identical or similar elements. It should be understood that these drawings are not necessarily drawn to scale. They are presented just for illustrative purposes only, and are not intended to limit the scope of the disclosure. Examples of materials, dimensions, and constructions are included for some elements. Those of ordinary skill in the art should understand that many of the examples provided have suitable alternatives and these alternatives should also be considered within the scope of this disclosure. Moreover, certain terminology is used herein for convenience only and is not to be taken as a limitation on the present disclosure.

FIG. 1 refers to a schematic representation of a device or system in accordance with one aspect of the present disclosure. The device or system comprises a de circuit and a RF circuit, each of which will be illustrated in more details below.

The de circuit in accordance with FIG. 1 includes a high voltage dc electrical source 1, a de power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 9. The electrode 7 is configured to be connectable to the high voltage dc electrical source 1 through an insulated conductor or wiring line 101. The insulated conductor or wiring line 101 may just be an insulated cable line. All the subsequent descriptions of these insulated conductor or wiring lines are expressed as cable lines or just cables for convenience unless explicitly expressed otherwise. The de power controller 2 may be placed between the dc electrical source 1 and the electrode 7. It may also be placed in cable line 102 to connect with the dc electrical source 1. It may also be placed between the cable line 101 and cable line 102 as shown in the FIG. 1. Generally, the de power controller 2 may be placed anywhere in the de circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the dc circuit even though FIG. 1 shows it is placed between the de power controller 2 through cable 103 and the electrode 9 through cables 104 and 107. Consequently, FIG. 1 illustrates a de circuit comprising the dc electrical source 1, the de power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 2, and cables 101, 102, 103, 104 and 107 as the functional portion of the dc circuit to perform smoke particle ionization and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the de circuit may also contain as many switches or controls as necessary to control or monitor the de circuit during a surgical operation.

The high voltage dc electrical source 1 in accordance with FIG. 1 may be from a main power supply for the generation of the high voltage necessary for ionization of debris. But it may be replaced or supplemented by a rechargeable storage battery. The high voltage dc electrical source 1 may be constant or interrupted by a switch operable by a surgeon or his/her assistant, for example a thumb operated switch or a foot pedal, to provide manual control (not shown in FIG. 1).

The de power controller 2 is included to control or monitor the current or voltage in the dc circuit. It will, for example, stop the current flow very quickly should the current increase rapidly in a short span of time. This will avoid or reduce accidental voltage shocks to the subject under a surgical procedure or operation. Additionally, it is possible to monitor increased impedance, and thereby detect a blocked electron emission. The do power controller can be placed anywhere in the de circuit as indicated above.

The RF isolation transformer 3 is incorporated into the circuit to make sure any RF current is eliminated during the de ionization process to safeguard the safety of the subject under the surgical procedure or operation. It can be placed anywhere in the de circuit as indicated above. Preferably, it may be placed close to the de electrical source. The RF isolation transformer may be selected from those commercially available such as Jensen transformers, Kramer transformers and others. A selection of a de power controller or a RF isolation transformer should be well within the ambit of a person of ordinary skill in the art.

The device is operable in an electrostatic configuration, which when connected, for example, through a plug-socket mechanism, to the negative pole of the high voltage de electrical source 1, the electrode 9 serves as the ionizing power to negatively charge the particles generated at or around a surgical site. In keeping with accepted theory, it sends a stream of electrons toward the atoms of the debris causing the atoms to form negative ions and thereby becoming attracted to the positively charged electrode 7. Under this situation, the electrode 9 may be made with a sharp tip or may include a shield and a tip such as disclosed in the US application publication No. 2012/0,067,212. The electrode 9 may also be made to include a positively charged accelerator ring. The accelerator ring improves the performance of the electrode 9 by drawing ions in the direction of their intended flow, in this case towards the electrode 7. The electrode 9 may further be made to have a conductive rod having a tip and a shield. The shield may terminate in a coiled spring-like formation covering the tip and protecting the subject from unintended trauma caused by the tip when in use. In one version the spring is not conductive and acts solely as a shield for said protection which can retract on insertion to expose the tip, whereas in another version the spring may be conductive to improve the performance of the electrode in producing electrons, but need not be retractable to expose the tip. In this latter configuration, it is the coiled formation that releases the electrons to form ions as disclosed in the US application publication No. 2012/0,067,212.

In the electrostatic configuration as described above, when the electrode 9 is connected to the negative pole of the high voltage de electrical source, the electrode 7 is then connected to the positive pole of the high voltage de electrical source to serve as a smoke particle attracting or collecting patch. The electrode 7 should accordingly be made to have a large surface area to facilitate collection of the negatively charged particles. The electrode 7 may also be made to increase its surface area through disposition over other electrodes in the RF circuit such as electrode 8 and electrode 10 which will be discussed in later paragraphs. It will be understood that insulating materials are needed to separate these electrodes to prevent them from interfering with each other. Methods of placing or mounting one electrode over another electrode are well known in the art, for example, as disclosed in U.S. Pat. Nos. 3,970,088 and 6,942,662.

The electrode 7 may be configured to be connectable with the dc electrical source 1 similarly through a plug/socket mechanism. For example, a plug may be extended from the dc source 1 through an insulated cable line to the electrode 7. Alternatively, a plug may be extended from the electrode 7 through an insulated cable line to connect with the dc source 1.

The RF circuit in accordance with FIG. 1 includes a surgical radio frequency energy generator 5, a third electrode 10, a fourth electrode 8, and a switch 4. The RF circuit in accordance with FIG. 1 may also include the second electrode 9 of the de circuit described above and configured to be connectable to the RF circuit through the switch 4. Further included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. The fourth electrode 8 is configured to be connectable to the RF generator 5 through the switch 4 by cables 105 and 106. The third electrode 10 is configured to be connectable to the RF generator 5 through cable 108. Accordingly, FIG. 1 illustrates a RF circuit of an electrosurgical configuration comprising the surgical RF generator 5, a RF controller (not shown), the switch 4, the electrode 8, the electrode 9, the electrode 10, and cables 105, 106, 107 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

In the electrosurgical configuration, by manipulating the switch 4, the generator 5, electrode 9, electrode 10 and the corresponding cables may cooperate to complete a first monopolar electrical circuit so that the device is operable as a first monopolar device. For example, electrode 9 may be an electrosurgical cut blade, and electrode 10 may be a remote electrode and/or pad. In the electrosurgical configuration, the switch 4 may be manipulated so that the generator 5, electrode 9, electrode 10 and the corresponding cables may cooperate to complete a first bipolar electrical circuit so that the device is operable as a first bipolar device. For example, electrode 9 and electrode 10 may be arms of a forceps device. In the electrosurgical configuration, the switch 4 may be manipulated so that the generator 5, electrode 10, the electrode 8, and the corresponding cables may cooperate to complete a second bipolar electrical circuit so that the device is operable as a second bipolar device. For example, electrode 8 and electrode 10 may be arms of a forceps device. Electrode 9 may be electrically disconnected from the surgical radio frequency energy generator 5, and may be a non-electrically charged cut blade (e.g., a cold cut blade). Alternatively, electrode 8 may be a bipolar electrosurgical cut blade in cooperation with electrode 10.

The surgical RF energy generator 5 should have a frequency of between 100 KHz and 100 MHz. More preferable, the frequency should be between 300 kHz and 2 MHz. This type of surgical RF energy generator is well understood by a person skilled in the art either for tissue cutting, cauterization, sealing or coagulation. The RF controller is included to monitor and/or control the RF output for different purposes such as cutting, coagulation or sealing. Additional RF controllers may also be included in the RF circuit to control or monitor the RF circuit to guarantee the safety of the subject under a surgical procedure or operation. This type of RF controller is also well understood and known by a skilled person in the art.

The switch 4 in accordance with FIG. 1 may be in the form of knobs, touches, slides, push buttons, magnetic or even remote type of controls, which are all within the grasp of a skilled person in the art. It may also be in the form of a computer or a computerized tool. The switch 4 in the RF circuit may, for example, be designed in a manner as disclosed in the U.S. Pat. Nos. 5,472,442, 5,312,327 and PCT application publication No. WO2014/151,560.

In accordance with FIG. 1, both the electrodes 8 and 10 are configured to be capable of performing tissue coagulation or sealing. Consequently, these two electrodes may be made to possess larger surface area in comparison with the electrode 9 which should be made to possess small surface area since it is configured to be used as a cutting blade in the RF circuit. Additionally, a connecting point 12 is configured to connect the electrode 9 into the RF circuit through the switch 4 through cable 107. Cable 104 may be lumped into cable 107 to form a single cable line for easy manipulation. It should be understood that the design of this type of cable connections is well known by a skilled person in the art.

As shown in FIG. 1 when connected to the surgical RF energy generator 5 through the switch 4, the electrode 8 may form a bipolar scaling or coagulating device with the electrode 10. Therefore, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. When connected to the surgical RF energy generator 5 through the switch 4, the electrode 9 may be used as a cutting blade and the electrode 10 may be used as a return current pad in the RF circuit. Consequently, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The electrode 9 may be configured to be connectable to the RF circuit through the switch 4. The electrode 9 may be switched on or off the RF circuit through the switch 4 depending on the need of the situation. The switch 4 may be configured to enable the electrode 9 to perform tissue cutting and to enable the electrodes 8 and 10 to perform tissue sealing or coagulation at the same time. Consequently, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting and coagulation at a surgical site of a subject. The dc circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting and/or coagulation. The materials and methods suitable for making the electrodes 8, 9 and 10 are well understood in the art for tissue cutting, sealing or coagulation, for example as disclosed U.S. Pat. Nos. 4,862,890, 4,958,539, 8,357,155, and 8,852,183.

Consequently, a device or system in accordance with FIG. 1 may be used as a monopolar cutting device, a bipolar cutting device, and/or a bipolar sealing or coagulating device in addition to being used as a smoke particle collector and/or extractor. It is contemplated that the device or system may perform tissue cutting and/or coagulation and smoke extraction simultaneously, concurrently, alternatively, intermittently, or sequentially.

Further in accordance with FIG. 1, the block 11 containing the electrodes 7, 8, 9 and 10 may be configured to form an insertable front portion of the device or system. Selections of size and/or dimension and/or material of the electrodes 7, 8, 9, and 10 each for their respective roles as cutting, sealing or coagulating, ionizing, or particle collecting are within the grasp of a killed person in the art. For example, the electrode 9 should be made narrow and sharp if it is to be used as a cutting blade in the RF circuit so that it can have high current density for an efficient cut, and it will also serve its purpose to be used as an ionizing source in the dc circuit. As for the electrode 7, on the contrary, it is to be made to possess a large surface area if it is to be used to attract and collect negatively charged particles. The electrode 7 or the electrode 9 may be configured to be connectable to the dc electricity source through a separate plug/socket system. Or, they may be bundled together by cables 101, 104, and 107 to form an integrated plug/socket system to connect with the dc circuit. The block 11 may also include switch 4 in the handle portion of the device for easy and convenient operation by the operator.

In accordance with FIG. 1, the block 6 containing the de power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 11 through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

When a device or system in accordance with FIG. 1 is put into use, the following steps are contemplated: connecting the electrodes 7 and 9 with the de electrical source 1 properly; checking to make sure the do power controller 2, the RF isolation transformer 3 and any other switches and/or controls in the de circuit are all in good and safe working conditions; properly connecting the switch 4 to the electrode 9 when performing tissue cutting; checking to make sure the RF controller and any other switches and/or controls in the RF circuit are all in good and safe working conditions; inserting the block 11 portion into its intended place where a surgical procedure or operation is desired; and then properly switching on the RF circuit to perform tissue cutting and/or tissue sealing and properly switching on the de circuit to ionize and to collect debris generated at a surgical site. Similarly, properly connecting the electrodes 8 and 10 through the switch 4 when performing tissue scaling or coagulation is desired. Likewise, properly connecting the electrodes 8, 9, and 10 through the switch 4 when both performing tissue cutting and performing tissue sealing or coagulation are desired. These steps may be repeated as many times as necessary. The dc circuit and the RF circuit may be switched on simultaneously, concurrently, alternatively, intermittently, or sequentially.

FIG. 2 shows a variation of a device or system in accordance with one aspect of the present disclosure. The device or system in accordance with FIG. 2 shares substantial similarities with a device or system of FIG. 1 except that the high voltage do source 1 is configured to be disposed in the block 11 where all the electrodes are disposed. In this embodiment, the do power source 1, for example, may be provided by a battery pack. The battery pack may be detachable from the device and may be rechargeable. The do power source 1 may be disposed in the handle portion or hand piece of the device. The electrodes 7, 8, 9 and 10 may be configured to be disposed in the front portion of the device. The electrodes 7, 8, 9 and 10 may be configured to form the insertable portion of the device or system. The device or system in accordance with FIG. 2 may be used in substantially similar ways as described above for FIG. 1 such as for monopolar and/or bipolar cutting and/or bipolar tissue sealing or coagulation. A device in accordance with FIG. 2 may be made portable such that all the electrodes are disposed in the front portion of the device and the de power source is disposed in the handle portion. The device or system in accordance with FIG. 2 may be connectable with a surgical RF generator through a plug/socket system or other means well known in the art.

FIG. 3 shows another variation of a device or system in accordance with one aspect of the present disclosure. A device or system in accordance with FIG. 3 shares many similarities with a device of FIG. 1 or FIG. 2. The significant difference comes from the fact that one of the two sealing or coagulating electrodes is incorporated into the de circuit instead of the cutting blade (i.e., identified as electrode 9 as in FIG. 1 or FIG. 2). Additionally, the sealing electrode can be switched off the do circuit through the switch 4. When that happens, the cutting electrode 9 and the other sealing electrode 10 may form a tissue cutting device in the RF circuit to cut tissues when connected to the surgical RF generator 5. When connected with the surgical RF energy source 5 through the switch 4 as shown in FIG. 3, the electrode 8 may form a bipolar sealing or coagulation device with the electrode 10 to perform tissue sealing or coagulation. Consequently, a device of FIG. 3 may be used as a bipolar cutting device or a bipolar sealing device substantially similar to a device of FIG. 1 or FIG. 2. Also similar to a device or system of FIG. 2 in that the high voltage dc source 1 is disposed in the same block 1I as all the electrodes, the dc power source 1 may accordingly be provided by a battery pack. The battery pack may be detachable from the device and may be rechargeable. The de power source may be configured to be in the handle portion or hand piece of the device. The electrodes 7, 8, 9 and 10 may be configured to be disposed in the front portion of the device. The electrodes 7, 8, 9 and 10 may be configured to form the insertable portion of the device.

FIG. 4 shows another variation of a device or system in accordance with one aspect of the present disclosure. A device in accordance with FIG. 4 shares many similarities with a device of FIG. 3. In particular, both the device of FIG. 4 and the device of FIG. 3 use one of the two RF sealing or coagulating electrodes (i.e., electrode 8 in FIG. 3 and electrode 10 in FIG. 4), in the dc circuit. A device or system in accordance with FIG. 4, however, is configured to incorporate the non-switchable sealing electrode 10 into the dc circuit, meaning the electrode cannot be switched off the dc circuit by the switch 4. Instead, it is a fixed part of the RF circuit. Consequently, when connected with the electrode 8 through the switch 4, the electrode 10 may form a bipolar tissue sealing or coagulation device in the RF circuit. Yet when connected with the electrode 9 through the switch 4, the electrode 10 may form a monopolar or bipolar tissue cutting device in the RF circuit. As a result, a device or system of FIG. 4 may be used as a monopolar or bipolar cutting device or a bipolar sealing device substantially similar to a device of FIG. 1, FIG. 2, or FIG. 3. Also similar to a device or system of FIG. 2 or FIG. 3 in that the high voltage dc source 1 is disposed in the same block 11 as the electrodes 7, 8, 9 and 10, the de power source 1 may accordingly be provided by a battery pack. The battery pack may be detachable from the device and may be rechargeable. The dc power source may be configured to be disposed in the handle portion or hand piece of the device. The electrodes 7, 8, 9 and 10 may be configured to be disposed in the front portion of the device. A device in accordance with FIG. 4 may be similarly operable as a device of FIG. 1, FIG. 2, or FIG. 3.

FIG. 5 shows another variation of a device in accordance with one aspect of the present disclosure. The device contains a de circuit and a RF circuit. The dc circuit includes a high voltage de electrical source 1, a dc power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 8. The electrode 7 is configured to be connectable to the high voltage de electrical source 1 through an insulated conductor or wiring line 101. As previously described, the dc power controller 2 may be placed anywhere in the de circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the de circuit even though FIG. 5 shows it is placed between the dc power controller 2 through cable 103 and the electrode 8 though cables 104 and 105. Consequently, FIG. 5 illustrates a de circuit comprising the de electrical source 1, the de power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 8, and cables 101, 102, 103, 104 and 105 as the functional portion of the de circuit to perform smoke particle ionization, collection, and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the dc circuit of FIG. 7 performs smoke particle ionization, attraction, reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the de circuit may contain as many switches or controls as necessary to control or monitor the dc circuit.

The RF circuit in accordance with FIG. 5 includes a surgical radio frequency energy generator 5, the electrode 8, and a third electrode 10. As a result, the electrode 8 is included both in the dc circuit and in the RF circuit. Also included in the RF circuit is at least a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. The third electrode 10 is connected to the surgical RF generator 5 through cable 108. The electrode 8 is connected to the surgical RF generator 5 through cables 105 and 106. Accordingly, FIG. 5 illustrates a RF circuit comprising the RF generator 5, a RF controller (not shown), the electrode 8, the electrode 10, and cables 105, 106, and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 5, when connected to the RF surgical RF energy generator 5 through cables 105 and 106, the electrode 8 may form a bipolar cutting, or sealing or coagulating device with the electrode 10. Therefore, the dc circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. The de circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue sealing or coagulation.

In accordance with FIG. 5, the block 11 containing the electrodes 7, 8, and 10 may be configured to form an insertable front portion of the device or system. Selections of size and/or dimension and/or material of the electrodes 7, 8, and 10 each for their respective roles as sealing or coagulating, ionizing, or collecting are within the grasp of a killed person in the art. For example, the electrode 7 should be made narrow and sharp if it is to be used as an ionizing source in the de circuit. As for the electrode 8, on the contrary, it is to be made to possess a large surface area if it is to be used to attract and collect negatively charged particles. The electrode 7 or the electrode 8 may be configured to be connectable to the de electricity source through a separate plug/socket system. Or, they may be bundled together by cables 101 and 104 and 105 to form an integrated plug/socket system to connect with the dc circuit. Moreover, since the high voltage dc electrical source 1 shares the same block with the electrodes 7, 8, and 10, the de electrical source 1, for example, may be provided by a battery pack. The battery pack may be detachable from the device and may be rechargeable. The do electrical source 1 may be configured to be disposed in the handle portion or hand piece of the device. The electrodes 7, 8, and 10 may be configured to be disposed in the front portion of the device.

FIG. 6 shows another variation of a device in accordance with one aspect of present disclosure. The device in accordance with FIG. 6 shares substantial similarities with a device of FIG. 5 except that the high voltage dc source 1 of FIG. 6 is separately disposed in the block 6 instead of the block 11. As a result, the connection of the block 11 containing the electrodes 7 and 8 in the dc circuit with the block 6 containing the de electrical source 1 may be through a plug/socket mechanism, or through some other mechanisms known in the art. Also, the block 11 containing the electrodes 7, 8, and 10 may be configured to be disposed in the front portion of the device. The electrodes 7, 8, and 10 may be configured to form an insertable portion of the device. A device in accordance with FIG. 6 may be made portable such that all the electrodes are disposed in the front portion of the device and that it is connectable with a RF generator through a plug/socket system or other means well known in the art.

The device or system in accordance with FIG. 6 may be used in substantially similar ways as described for a device of FIG. 5. It may be particularly suitable for removing or reducing debris generated during bipolar tissue sealing or coagulation by the device.

FIG. 7 shows another variation of a device or system in accordance with one aspect of the present disclosure. The device contains a do circuit and a RF circuit. The de circuit includes a high voltage dc electrical source 1, a dc power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 8. The electrode 7 is connected to the high voltage de electrical source 1 through an insulated conductor or wiring line 101. As described previously, the de power controller 2 may be placed anywhere in the dc circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the dc circuit even though FIG. 7 shows it is placed between the de power controller 2 through cable 103 and the electrode 8 through cables 104 and 105. Consequently, FIG. 7 illustrates a do circuit comprising the dc electrical source 1, the dc power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 8, and cables 101, 102, 103, 104 and 105 as the functional portion of the dc circuit to perform smoke particle ionization and attraction, removal or reduction of the ionized debris generated at a surgical site. It will be understood that the de circuit of FIG. 7 performs smoke particle reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the dc circuit may contain as many switches and/or controls as necessary to control or monitor the do circuit.

The RF circuit in accordance with FIG. 7 includes a surgical radio frequency energy generator 5, a RF current return pad 13, and the electrode 8. As a result, the electrode 8 is incorporated into both the dc circuit and the RF circuit as well. Also included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. Accordingly, FIG. 7 illustrates a RF circuit (i.e., a first monopolar electrical circuit) comprising the RF generator 5, a RF controller (not shown), the electrode 8, the RF current return pad 13, and cables 105, 106, and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 7, when connected to the RF surgical RF energy generator 5 through cables 105 and 106, the electrode 8 may form a first monopolar device in the form of a monopolar cutting device with the RF current return pad or electrode 13. The electrode 13 may be remote from the surgical site. The electrode 13 may be applied to the exterior skin of the patient so that the ionized particles are attracted to the body of the patient. The electrode 13 may plug into a dedicated return plug on the generator 5. This description of electrode 13 may refer to any of the other configurations described in this disclosure when referring to an electrode that is a remote electrode pad or return electrode. Therefore, the dc circuit may be turned on to ionize, attract, remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The de circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting.

FIG. 8 shows another variation of a device or system in accordance with one aspect of the present disclosure. The device contains a dc circuit and a RF circuit. The do circuit includes a high voltage de electrical source 1, a dc power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 13. The electrode 7 is configured to be connectable to the high voltage do electrical source 1 through an insulated conductor or wiring line 101. As described previously, the dc power controller 2 may be placed anywhere in the dc circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the dc circuit even though FIG. 8 shows it is placed between the do power controller 2 through cable 103 and the electrode 13 through cable 104. Consequently, FIG. 8 illustrates a de circuit comprising the dc electrical source 1, the dc power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 13, and cables 101, 102, 103, and 104 as the functional portion of the dc circuit to perform smoke particle ionization, attraction, and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the dc circuit of FIG. 8 performs smoke particle attraction, reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the de circuit may contain as many switches or controls as necessary to control or monitor the de circuit.

The RF circuit in accordance with FIG. 8 includes a radio frequency energy generator 5, a third electrode 8, and the electrode 13. As a result, the electrode 13 is configured to be included both in the de circuit and in the RF circuit. More particularly, the electrode 13 in accordance with FIG. 8 is configured to be an ionized particle collecting patch in the dc circuit and a RF current return pad or remote electrode pad in the RF circuit. Also included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. Accordingly. FIG. 8 illustrates a RF circuit or monopolar electrical circuit comprising the RF generator 5, a RF controller (not shown), the electrode 8, the RF current return pad or remote electrode pad 13, and cables 105, and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 8, when connected to the RF surgical RF energy generator 5 through cable 105, the electrode 8 may form a monopolar cutting device with the RF current return pad or remote electrode pad 13. Therefore, the de circuit may be turned on to attract, remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The do circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting.

FIG. 9 shows another variation of a device or system in accordance with one aspect of the present disclosure. The device contains a do circuit and a RF circuit. The de circuit of FIG. 9 includes a high voltage de electrical source 1, a dc power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 13. The electrode 7 is configured to be connectable to the high voltage dc electrical source 1 through an insulated conductor or wiring line 101. As described previously, the dc power controller 2 may be placed anywhere in the dc circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the de circuit even though FIG. 9 shows it is placed between the dc power controller 2 through cable 103 and the electrode 13 through cable 104. Consequently, FIG. 9 illustrates a do circuit comprising the dc electrical source 1, the dc power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 13, and cables 101, 102, 103 and 104 as the functional portion of the dc circuit to perform smoke particle ionization, attraction, and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the do circuit of FIG. 9 performs smoke particle reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the dc circuit may contain as many switches or controls as necessary to control or monitor the de circuit.

The RF circuit in accordance with FIG. 9 includes a radio frequency energy generator 5, an electrode 8, and an electrode 10. Also included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. Accordingly, FIG. 9 illustrates a RF circuit comprising the RF generator 5, a RF controller (not shown), the electrode 8, the electrode 10, and cables 105 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 9, when connected to the surgical RF energy generator 5 through cable 105, the electrode 8 may form a bipolar tissue sealing or coagulation device with the electrode 10. Therefore, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. The dc circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue sealing or coagulation.

In accordance with FIG. 9, the block 11 containing the electrodes 7, 8, and 10 may be configured to form an insertable front portion of the device or system. Selections of size and/or dimension and/or material of the electrodes 7, 8, and 10 each for their respective roles as sealing or coagulating, or ionizing are within the grasp of a skilled person in the art. For example, the electrode 7 should be similarly made as the electrode 9 of a device of FIG. 1 for the purpose as an ionizing electrode in the dc circuit. As for the electrode 13, on the contrary, it is to be made to possess a large surface area to attract and collect negatively charged particles.

In accordance with FIG. 9, the block 6 containing the de power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 1I through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

FIG. 10 shows another variation of a device or system in accordance with one aspect of the present disclosure. The device contains a dc circuit and a RF circuit. The de circuit of FIG. 10 includes a high voltage de electrical source 1, a dc power controller 2, a RF isolation transformer 3, a first electrode 7, and a second electrode 8. The electrode 7 is configured to be connectable to the high voltage dc electrical source 1 through an insulated conductor or wiring line 101. As previously described, the de power controller 2 may be placed anywhere in the dc circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the dc circuit even though FIG. 10 shows it is placed between the dc power controller 2 through cable 103 and the electrode 8 through cables 104 and 107. Consequently, FIG. 10 illustrates a de circuit comprising the de electrical source 1, the dc power controller 2, the RF isolation transformer 3, the first electrode 7, the second electrode 8, and cables 101, 102, 103, 104, and 107 as the functional portion of the de circuit to perform smoke particle ionization, attraction, and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the dc circuit of FIG. 10 performs smoke particle reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the de circuit may contain additional switches or controls as necessary to control or monitor the de circuit.

The RF circuit in accordance with FIG. 10 includes a radio frequency energy generator 5, a third electrode 10, and the electrode 8. As a result, the electrode 8 is configured to be included both in the de circuit and in the RF circuit. Further included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. Accordingly, FIG. 10 illustrates a RF circuit comprising the RF generator 5, a RF controller (not shown), the electrode 8, the electrode 10, and cables 106, 107 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject. It will be understood that the RF circuit may also contain additional switches or controls as necessary to control or monitor the RF circuit.

As shown in FIG. 10, when connected to the surgical RF energy generator 5 through cables 105 and 107, a bipolar electrical circuit is completed and the electrode 8 may form a bipolar tissue cutting, sealing or coagulation device with the electrode 10. Therefore, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. The dc circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue sealing or coagulation.

In accordance with FIG. 10, the block 11 containing the electrodes 7, 8, and 10 may be configured to form an insertable front portion of the device or system. Selections of size and/or dimension and/or material of the electrodes 7, 8, and 10 each for their respective roles as scaling or coagulating, ionizing, or particle collecting are within the grasp of a skilled person in the art. For example, the electrode 7 may be similarly made as the electrode 9 of a device of FIG. 1 if it is to be used as an ionizing electrode in the de circuit. As for the electrode 8, on the contrary, it should be made to possess a large surface area if it is used to attract and collect negatively charged particles in the de circuit.

In accordance with FIG. 10, the block 6 containing the do power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 11 through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

It will be appreciated that when a device in accordance with FIG. 10 is put into use, the specific steps of using it are contemplated to be similar to those previously described, or may be easily adapted based on previous embodiments of the present disclosure.

FIG. 11 shows another variation of a device or system in accordance with one embodiment of the present disclosure. The device contains a do circuit and a RF circuit. The do circuit includes a high voltage do electrical source 1, a do power controller (not shown), a RF isolation transformer (not shown), a first electrode 7, and a second electrode 14. The electrode 7 is configured to be connectable to the high voltage de electrical source 1 through an insulated conductor or wiring line 101. As previously described, the de power controller may generally be placed anywhere in the de circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer may also be placed anywhere in the de circuit. Consequently, FIG. 11 illustrates a de circuit comprising the dc electrical source 1, the first electrode 7, the second electrode 14, and cables 101 and 102 as the functional portion of the de circuit to perform smoke particle ionization and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the dc circuit of FIG. 11 performs smoke particle ionization, attraction, reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the dc circuit may contain as many additional switches or controls as necessary to control or monitor the dc circuit.

The RF circuit in accordance with FIG. 11 includes a radio frequency energy generator 5, electrode 8, electrode 9, electrode 10, and a switch 4. Also included in the RF circuit is a capacitor 19 between the electrode 8 and the electrode 10. The capacitor allows the energy to go through to the electrode tips depending on the output of the capacitor. The function of this capacitor is well understood in the art. Further included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. The electrode 8 is configured to be connectable to the RF generator 5 through the switch 4 by cables 105 and 106. The electrode 9 is also configured to be connectable to the RF generator 5 through the switch 4 by cables 107 and 106. Accordingly, FIG. 11 illustrates a RF circuit comprising the RF generator 5, a RF controller (not shown), the switch 4, the electrode 8, the electrode 9, the electrode 10, the capacitor 19, and cables 105, 106, 107 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 11 when connected to the surgical RF energy generator 5 through the switch 4, the electrode 8 may form a bipolar cutting sealing or coagulating device with the electrode 10. Therefore, the dc circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. When connected to the surgical RF energy generator 5 through the switch 4, the electrode 9 may be used as a cutting blade and the electrode 10 may be used as a return current pad or remote electrode pad in the RF circuit. Consequently, the dc circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The switch 4 may be configured to enable the electrode 9 to perform tissue cutting and to also enable the electrodes 8 and 10 to perform tissue sealing or coagulation at the same time. Consequently, the dc circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting and coagulation at a surgical site of a subject. The dc circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting or the coagulating.

In accordance with FIG. 11, the block 11 containing the electrodes 7, 8, 9 and 10 may be configured to form an insertable front portion of the device or system. Again, the materials and methods suitable for making the electrodes 7, 8, 9 and 10 are well understood in the art for tissue cutting, sealing or coagulation as similarly described for a device of FIG. 1.

In accordance with FIG. 11, the block 6 containing the dc power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 11 through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

FIG. 12 shows another variation of a device or system in accordance with one embodiment of the present disclosure. The device contains a de circuit and a RF circuit. The de circuit includes a high voltage de electrical source 1, a dc power controller (not shown), a RF isolation transformer 3, a first electrode 7, and a second electrode 9. The electrode 7 is configured to be connectable to the high voltage de electrical source 1 through an insulated conductor or wiring line 101. As previously described, the do power controller may generally be placed anywhere in the dc circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer may also be placed anywhere in the do circuit even though FIG. 12 shows it is placed between the electrode 9 and the dc electrical source 1. Consequently, FIG. 12 illustrates a dc circuit comprising the dc electrical source 1, the first electrode 7, the second electrode 9, and cables 101, 103, 104, and 107 as the functional portion of the dc circuit to perform smoke particle ionization and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the dc circuit of FIG. 12 performs smoke particle reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the do circuit may contain as many additional switches or controls as necessary to control or monitor the de circuit.

The RF circuit in accordance with FIG. 12 includes a radio frequency energy generator 5, a third electrode 10, a fourth electrode 8, a switch 4, and the second electrode 9. Consequently, the electrode 9 is configured to be included both in the dc circuit and in the RF circuit. More particularly, it is configured to be connectable with the RF circuit through the switch 4. Also included in the RF circuit is a capacitor 19 placed between the electrode 8 and the electrode 10. Further included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. The electrode 8 is configured to be connectable to the surgical RF energy generator 5 through the switch 4 by cables 105 and 106. Accordingly, FIG. 12 illustrates a RF circuit comprising the surgical RF energy generator 5, a RF controller (not shown), the switch 4, the electrode 8, the electrode 9, the electrode 10, the capacitor 19, and cables 105, 106, 107 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 12 when connected to the surgical RF energy generator 5 through the switch 4, a bipolar electrical circuit is completed so that the electrode 8 may form a bipolar sealing or coagulating device with the electrode 10. Therefore, the dc circuit may be turned on to attract, remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. When connected to the surgical RF energy generator 5 through the switch 4, a monopolar or bipolar electrical circuit may be completed so that the electrode 9 may be used as a cutting blade and the electrode 10 may be used as a return current pad or electrode or remote electrode pad in the RF circuit. Consequently, the do circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The de circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting or the coagulating.

In accordance with FIG. 12, the block 11 containing the electrodes 7, 8, 9 and 10 may be configured to form an insertable front portion of the device or system. Again, the materials and methods suitable for making the electrodes 7, 8, 9 and 10 are well understood in the art for tissue cutting, sealing or coagulation, ionization, or particle collection as similarly described for a device of FIG. 1.

In accordance with FIG. 12, the block 6 containing the dc power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 11 through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

FIG. 13 shows another variation of a device or system in accordance with one aspect of the present invention. The device contains a de circuit and a RF circuit. The dc circuit includes high voltage de electrical source 1, a de power controller (not shown), a RF isolation transformer 3, a first electrode 7, a second electrode 8, and a third electrode 10. The electrode 7 is configured to be connectable to the high voltage de electrical source 1 through an insulated conductor or wiring line 101. As previously described, the de power controller may be placed anywhere in the de circuit so long as it can effectively and efficiently control the voltage and/or current whenever it is needed or desirable. Similarly, the RF isolation transformer 3 may also be placed anywhere in the de circuit even though FIG. 13 shows it is placed between the de electrical source 1 through cable 103 and the electrodes 8 and 10 through cable 104. Consequently, FIG. 12 illustrates a dc circuit comprising the de electrical source 1, the first electrode 7, the second electrode 8, the third electrode 10, and cables 102, 103, 104, and 105 as the functional portion of the de circuit to perform smoke particle ionization, attraction, and removal or reduction of the ionized debris generated at a surgical site. It will be understood that the de circuit of FIG. 13 performs smoke particle reduction or removal in ways similar to what was previously described for FIG. 1. It will also be understood that the de circuit may contain as many additional switches or controls as necessary to control or monitor the de circuit.

The RF circuit in accordance with FIG. 13 includes a radio frequency energy generator 5, a fourth electrode 9, the second electrode 8, the third electrode 10, and a switch 4. As a result, both the electrode 8 and the electrode 10 are configured to be included in the de circuit and in the RF circuit as well. Also included in the RF circuit is a capacitor 19 between the electrode 8 and the electrode 10. Further included in the RF circuit is a RF current and voltage controller (not shown) which may be placed any place in the RF circuit. The electrode 8 is configured to be connectable to the RF generator 5 through the switch 4 by cables 105 and 106. The electrode 9 is also configured to be connectable to the RF generator 5 through the switch 4 by cables 107 and 106. Accordingly. FIG. 13 illustrates a RF circuit comprising the RF generator 5, a RF controller (not shown), the switch 4, the electrode 8, the electrode 9, the electrode 10, the capacitor 19, and cables 105, 106, 107 and 108 as the functional portion of the RF circuit to perform a surgical procedure or operation on a subject.

As shown in FIG. 13 when connected to the surgical RF energy generator 5 through the switch 4, the electrode 8 may form a bipolar sealing or coagulating device with the electrode 10. Therefore, the de circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue sealing or coagulation at a surgical site of a subject. When connected to the surgical RF energy generator 5 through the switch 4, the electrode 9 may be used as a cutting blade and the electrode 10 may be used as a return current pad or remote electrode pad in the RF circuit. Consequently, the dc circuit may be turned on to remove or reduce the debris when the RF circuit is switched on to perform tissue cutting at a surgical site of a subject. The de circuit may be turned on simultaneously, concurrently, alternatively, intermittently, or sequentially when the RF circuit is switched on to perform the tissue cutting or the coagulating.

In accordance with FIG. 13, the block 1 containing the electrodes 7, 8, 9 and 10 may be configured to form an insertable front portion of the device or system. The materials and methods suitable for making the electrodes 7, 8, 9 and 10 are well understood in the art for tissue cutting, sealing or coagulation, ionization, and particle collection as similarly described for a device of FIG. 1.

In accordance with FIG. 13, the block 6 containing the de power source 1 and the RF power source 5 may form separate parts configured to be connectable with the block 1 through a plug/socket system or other means that are well understood by a skilled person in the art. The plug/socket system may also include additional hand switches and/or foot pedals whenever desired or necessary.

FIG. 14 shows another variation of a device or system in accordance with one aspect of the present disclosure when it is desired to remove or reduce debris from a surgical site such as the abdomen of a subject. The system in accordance with FIG. 14 comprises a de circuit and a RF circuit. The dc circuit comprises a high voltage dc electrical source box 1, an electrode 9, and an electrode 7. The dc electrical source box 1 may be configured to include a dc electrical source, a current/voltage controller, and a RF isolation transformer. The box 1 may be configured to be disposed in the handle portion of the device, or it may be configured to be detachable from the device. The de circuit may be powered by a battery pack if the box 1 is configured to be disposed in the handle portion of the device. The RF circuit comprises a RF energy source 5, an electrode 10, a RF current return pad or remote electrode pad 13, the electrode 9, and a switch 4. As a result, the electrode 9 is configured to be in the dc circuit and also in the RF circuit as well. The electrodes 7, 9, and 10 are configured to form the insertable portion of the device. The device is inserted through a cannula (not shown) into a surgical site such as the abdomen region 201 of a subject. Additionally, both the de circuit and the RF circuit may contain additional switches or controllers as necessary to control or monitor the dc circuit and the RF circuit. The electrode 9 is to be made to possess a ship tip as similarly described for the electrode 9 of FIG. 1 in order to have efficient ionization capability. The electrode 7, configured to be a particle collecting patch for the ionized debris in the de circuit, is to be made to possess large surface area. FIG. 14 illustrates the electrode 7 is configured to cover the outer surface of the insertable portion of the device. The electrode 10 may be made to possess a large surface area since it may be configured as the return electrode in a bipolar cutting mode for the RF circuit.

When it is desired to use a device of FIG. 14 as a monopolar cutting device, the electrode 9 may be connected with the return patch 13 through the switch 4 to form a monopolar cutting device. The return current pad or remote electrode pad 13 may be placed under the outside skin of a subject. When it is desired to use a device of FIG. 14 as a bipolar cutting device, the electrode 9 may be connected with the electrode 10 also through the switch 4 to form a bipolar cutting device. The electrode 10 is then used as the return pad. Additionally, or alternatively, the electrode 9 may be configured to comprise two subset electrodes 9 a and 9 b. The electrode 9 a may be configured to be an ionization electrode and also a cutting blade. The electrode 9 b may be configured to form a bipolar sealing device with the electrode 10.

When it is desired to attract, remove or reduce debris from a surgical site such as the abdomen of a subject by a device of FIG. 14, the high voltage de supply box 1 can be switched on and a stream of electrons would then be generated around the tip of the electrode 9. The effect of these electrons around electrode 9 is to ionize any particles or matter suspended around the surgical site. Once the debris are ionized, they will be attracted to the positively charged patch 7. The de power supply box 1 may be turned on concurrently, simultaneously, sequentially, alternatively, or intermittently with the surgical procedure or operation.

FIG. 15 shows another variation of, a device in accordance with one aspect of the present disclosure when it is desired to remove or reduce debris from a surgical site such as the abdomen of a subject. More particularly, a device in accordance with FIG. 15 is a simplified representation of a stand-alone smoke extractor. The device contains a dc circuit comprising a dc power supply box 1 in which a high voltage dc electrical source is housed, a first electrode 8, and a second electrode 7. The electrode 7 is configured to cover the outer surface of the insertable portion of the device. The electrode 7 may be further covered with an outer layer with small holes or pores to allow ionized particles to get through the outer layer to be attracted to the electrode 7. The outer layer should be made with materials that will facilitate the extractor's insertion through a cannula, an access sheath or other tools to a surgical site such as the abdomen of a subject. The electrode 8 may be configured to be a circular electrode that is capable of ionizing debris at a surgical site after it is connected to a high voltage dc electrical source. The connecting line between the electrode 8 and the box 1 may be configured to not only electrically connect the electrode 8 with the dc power source box 1, but also to be strong enough to allow the electrode 8 to be movable along the longitudinal direction. The extractor optionally further comprises a filter 10 which may be used to filter debris.

The smoke extractor is insertable through a tool such as cannula into a surgical site such as the abdomen region 201 of a subject. The dc power supply box 1 may be configured to include a de electrical source, a RF isolation transformer, and a de voltage/current controller. Additionally, it may also contain other switches or controllers as necessary to monitor the de circuit.

FIG. 16 shows another variation of a device in accordance with one aspect of the present disclosure. The device contains a dc circuit comprising a first electrode 7, a second electrode 9, and wire conductors insulated from one another (not shown), extending through the lumen of the device (not shown) to form an insulating plug-like insert 31 which facilitates a coupling of the device with a high voltage de electrical source (not shown). The device also contains a RF circuit comprising a third electrode 8, a fourth electrode 10, and wire conductors insulated from one another (not shown), extending also through the lumen of the device to form an insulating plug-like insert 32 which facilitates a coupling of the device with an ac or surgical RF energy source (not shown). The switches or controllers for monitoring or controlling the dc circuit and/or the RF circuit may be disposed on the handle 30 (not shown). More particularly, a dc circuit controller, a RF isolation transformer may be disposed in the handle 30 portion.

In accordance with FIG. 16, the electrode 9 of the device is intended to be used as an ionizing electrode in the de circuit to ionize debris generated at a site of a surgical procedure or operation, while the electrode 7 is intended to be used to attract and to collect the ionized debris. Under this circumstance, the electrode 7 should be made to possess a large surface area. Consequently, the electrode 7 may be made to partially or wholly cover the outer surface of the tubular member of the device. The electrode 7 may be made with any known conductive materials suitable for such purpose such as nickel gauze which can be washed after use, a mat of conductive material such as random plastic fibers coated in conductive carbon slurry, or a metallic plate.

In accordance with FIG. 16, the electrode 9 of the device is also intended to be used as a cutting blade in the RF circuit. It may be configured to perform a monopolar cutting with an external return pad or remote electrode pad (not shown), or perform a bipolar cutting with either the electrode 8 or the electrode 10 or both as a return pad or remote electrode pad. The electrode 8 and the electrode 10 may be configured to perform bipolar tissue sealing or cauterization.

Additionally, or alternatively, a device in accordance with FIG. 16 may not need to have a plug-like insert 31 for coupling with a high voltage de electrical source if a battery pack is desired to be disposed inside the handle 30 to power the dc circuit (not shown). When a battery pack is contemplated to be disposed inside the handle 30, the first electrode 7 and the second electrode 9 may be connected to the battery pack through insulated wire conductors inside the lumen of the insertable portion of the device (not shown).

In accordance with FIG. 16, the electrodes 7, 8, 9, and 10 are configured to form the insertable portion of the device. Their sizes, dimensions, ratios and/or materials may be made in accordance with the specific needs of the device. Moreover, what is shown in FIG. 16 does not reflect their respective ratios or scales for those electrodes. It should rather be understood that they are merely for illustration purpose.

FIG. 17 illustrates an exemplary medical device 100. The device 100 may include any one of the electrode configurations illustrated and/or described herein. The electrodes are schematically identified as being located in area 103. Area 103 may be a distal end of an introducer 104 that may be at least partially inserted into a patient or site of interest during a surgical procedure. The introducer 103 may be connected to the hand piece 30. The ac or RF energy source 5 and the dc energy source 1 are contained in a single, common generator 36. The device 100 includes a single cord 33 and a single plug 31 for connecting to a receptacle 35 on the generator 35. The de energy and the ac energy is transferred between the generator 36 and the one or more electrodes via the single cord 33. As was discussed above, the de energy and the ac energy can be transferred simultaneously, concurrently, alternatively, intermittently, or sequentially. In some embodiments, the de energy may be transferred during or after a surgical procedure or operation.

FIG. 18 illustrates an exemplary medical device 100. The device 100 may include any one of the electrode configurations illustrated and/or described herein. The electrodes may be in the textured area 103 of FIG. 18. Area 103 may be a distal end of an introducer 104 that may be at least partially inserted into a patient or site of interest during a surgical procedure. The introducer 103 may be connected to the hand piece 30. The dc energy source is located in the hand piece 30. The device 100 includes a single cord 33 and a single plug 31 for connecting to a receptacle 35 on the ac or RF energy source 1. The ac energy is transferred between the energy source 1 and the one or more electrodes via the single cord 33. As was discussed above, the dc energy and the ac energy can be transferred simultaneously, concurrently, alternatively, intermittently, or sequentially. In some embodiments, the dc energy may be transferred during or after a surgical procedure or operation.

FIG. 19 illustrates an exemplary medical device 100. The device 100 includes an electrosurgical device 101 that includes one or more of the electrosurgical electrodes described and/or illustrated herein in the area 103. The electrosurgical electrodes are the electrodes for performing an electrosurgical procedure, such as monopolar or bi polar tissue cutting; monopolar or bipolar tissue coagulation, or both. The electrosurgical electrodes are connected to the ac or radio frequency source 5 via a single cord 33 having a plug 31 connecting to a socket 35 on the generator. The medical device 100 also includes an electrostatic device 102. The electrostatic device 102 is contained in a housing that can be attached or clipped-on to the electrosurgical device 101. The electrostatic device 102 comprises the electrodes described herein that are configured to ionize, attract, and/or remove the particles from the surgical site. The DC source 1 is contained in the electrostatic device 102. The electrostatic device 102 and/or the housing that contains the electrostatic device 102 may be removeably attached or clipped onto the electrosurgical device 101 such that device 102 can be attached, detached, and reattached one or more times without destroying either device 101, 102 or portions thereof. The dc source 1 may be located in the device 102, and may be attached and detached from the device 102 without destroying the functionality of the device 102 or the source 1.

FIG. 20 shows another variation of a device or system. The system includes a tubular introducer 104, which may be a portion of the device that can be inserted into the anatomy during a surgical procedure. The system in accordance with FIG. 20 comprises a dc circuit and a RF circuit. The dc circuit comprises a dc electrical source 1, a first electrode 7, and a second electrode 9. The second electrode 9 extends from a distal end of the introducer 104, and the first electrode 7 is located at or near the distal end of the introducer 104. The first electrode 7 can be located on an inner surface of the introducer 104 or the outer surface of the introducer 104. The de electrical source 1 may be configured to include a dc electrical source, a current/voltage controller, an RF isolation transformer, or a combination thereof. The dc electrical source 1 may be located in a handle portion of the device, or may be a separate component that is connected to the device via one or more cables. The AC or RF circuit comprises an AC or RF energy source 5, a third electrode 10, a fourth electrode that may be configured as an AC or RF current return pad or remote electrode pad 13, the second electrode 9, and a switch 4. The third electrode 10 extends from a distal end of the introducer 104. As a result, the second electrode 9 is configured to be in the de circuit and also in the RF circuit as well. The introducer 104 and/or the electrodes 7, 9, and 10 may be configured to form the insertable portion of an intracorporeal device.

The device of FIG. 20 may also include a filter 20. The filter 20 may be a sleeve that at least partially covers the first electrode 7. The device can be inserted through a cannula (not shown) into a surgical site such as the abdomen region 201 of a subject. However, it is understood that the device can be configured as an extracorporeal device for removing debris from an extracorporeal surgical site. Both the dc circuit and the AC or RF circuit may contain additional switches or controllers as necessary to control or monitor the de circuit and the RF circuit.

The first electrode 7 is electrically connected with a conductor wire to a pole of the DC electrical source, and the second electrode 9 is electrically connected with a conductor wire to a second pole of the DC electrical source. The first pole of the DC electrical source may be the positive pole, and the second pole of the DC electrical source may be the negative pole. In some configurations, the first pole of the DC electrical source may be the negative pole, and the second pole of the IX electrical source may be the positive pole. In any event, the electrodes 7, 9 are oppositely charged.

When it is desired to attract, remove or reduce debris from a surgical site such as the abdomen of a subject by a device of FIG. 20, the high voltage dc supply 1 can be switched on so that a stream of electrons is generated around the tip of the second electrode 9. The effect of these electrons around second electrode 9 is to ionize any particles or matter suspended around the surgical site. An electrical potential is created between the two electrodes 9, 7 so that the ionized particles or matter are attracted to or flow or travel from the second electrode 9 towards the first electrode 7.

The filter 20 is located between the two electrodes 9, 7 so that many, mostly, nearly all, or all of the ionized particles are restricted prevented from actually reaching the first electrode 7. Instead, many, mostly, nearly all, or all of the ionized particles are collected, captured, or arrested by the filter 20 so that the first electrode 9 remains clean and generally free of particles. This may ensure that the first electrode 9 continues to attract the ionized particles without the electrical potential or attraction weakening as may be the case if the ionized particles reach and cover the first electrode 7. Instead, when the filter 20 become saturated or dirty with particles, a user simply cleans or replaces the filter 20 without requiring the user to switch devices, or engage in a cumbersome and time consuming process of cleaning the first electrode 7.

In addition to preventing the debris from reaching the first electrode 7, the filter 20 may protect the first electrode 7 by collecting, restricting, and/or preventing liquids such as blood, saline, and/or other extracellular fluids from covering the first electrode 7, which may weaken or interfere with the strength of the particle attracting functions of the first electrode 7.

When it is desired to use a device of FIG. 20 as a monopolar cutting device, the second electrode 9 may be connected with the fourth electrode or the current return patch 13 through the switch 4 to form a monopolar cutting device. The fourth electrode or the current return patch 13 may be placed under the outside skin of a subject. When it is desired to use a device of FIG. 14 as a bipolar cutting device, the second electrode 9 may be connected with the third electrode 10 also through the switch 4 to form a bipolar cutting device. The third electrode 10 is then used as the return pad or remote electrode pad.

FIG. 21 shows schematic a device or system that includes a first electrode 7, a second electrode, and a de supply 1. The first electrode 7 is in electrical communication with the positive pole of the de supply 1 via an electrical conductor, and the second electrode 9 is in electrical communication with the negative pole of the dc supply 1 via an electrical conductor. When it is desired to attract and collect debris D from a surgical site, the high voltage de supply 1 can be switched on so that a stream of electrons is at the second electrode 9. The effect of these electrons around second electrode 9 is to ionize any debris D or matter suspended around the surgical site. An electrical potential is created between the two electrodes 9, 7 so that the ionized debris D or matter are attracted to or flow or travel from the second electrode 9 towards the first electrode 7. A filter 20 is disposed between the second electrode 9 and the first electrode 7. The electrical potential between electrodes 9, 7 extends through the filter 20 so that at least some if not all of the ionized debris D are collected and/or captured in the filter 20 as the ionized particles P or matter flow or travel towards the first electrode 7.

It should be understood that a device or system in accordance with any one embodiment as described above may also be arranged or adapted to reduce or remove debris from an extracorporeal surgical site. It may also be incorporated with other tools, devices or apparatus. Consequently, the present disclosure is not limited to only incorporate the surgical tools as described herein. It is contemplated that other surgical tools may be incorporated into the multifunctional device or system. Additionally, or alternatively, the multifunctional device described herein may be used in combination with other tools such as ultrasonic devices, laser devices and cryosurgical devices.

The contents of all references, patents, pending patent applications and published patents, cited throughout this application are hereby expressly incorporated by reference.

While preferred embodiments of the present disclosure have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will occur to those skilled in the art without departing from the disclosure. It should be understood that various alternatives to the embodiments of the disclosure described herein may be employed. It is intended that the following claims define the scope of the disclosure and that methods and structures within the scope of these claims and their equivalents be covered thereby. 

1. (canceled)
 2. A medical device comprising: a radio frequency (RF) circuit to perform a surgical procedure on the subject, the RF circuit including: a switch electrically coupled to a first pole of a source of surgical radio frequency (RF) energy; a first electrode electrically couplable to the first pole of the source of surgical RF energy via a first conductor and the switch; a second electrode electrically couplable to the first pole of the source of surgical RF energy via a second conductor and the switch; and a third electrode electrically couplable to a second pole of the source of surgical RF energy via a third conductor; and a DC circuit to ionize, and remove or reduce smoke particles generated at a surgical site on a subject, the DC circuit including: the first electrode, wherein the first electrode is electrically coupled to a first pole of a source of high voltage DC electricity via a fourth conductor; the second electrode, wherein the second electrode is electrically coupled to the first pole of the source of high voltage DC electricity via a fifth conductor; and a fourth electrode electrically coupled to a second pole of the source of high voltage DC electricity via a fifth conductor.
 3. The medical device of claim 2, wherein the DC circuit includes: an isolation transformer.
 4. The medical device of claim 3, wherein the isolation transformer is electrically coupled to the first pole of the source of high voltage DC electricity, the first electrode, and the third electrode.
 5. The medical device of claim 2, wherein when connected to the source of surgical RF energy through the switch, the first electrode forms a bipolar sealing or coagulating device with the third electrode.
 6. The medical device of claim 2, wherein when connected to the source of surgical RF energy through the switch, the second electrode forms a cutting blade and the third electrode forms a return current pad or a remote electrode pad.
 7. The medical device of claim 2, wherein the DC circuit and the RF circuit are configured to be operated concurrently with respect to one another.
 8. The medical device of claim 2, wherein the DC circuit and the RF circuit are configured to be operated intermittently with respect to one another.
 9. The medical device of claim 2, wherein the DC circuit and the RF circuit are configured to be operated alternatively with respect to one another.
 10. The medical device of claim 2, wherein the DC circuit and the RF circuit are configured to be operated simultaneously with respect to one another.
 11. The medical device of claim 2, wherein the DC circuit and the RF circuit are configured to be operated sequentially with respect to one another.
 12. The medical device of claim 2, wherein the medical device comprises: a handle member, and the source of high voltage DC electricity, wherein the source of high voltage DC electricity is located inside of the handle member.
 13. The medical device of claim 12, wherein the source of high voltage DC electricity is provided by a battery pack.
 14. The medical device of claim 2, wherein the source of high voltage DC electricity and the source of surgical RF energy are included in at least one first component block, wherein the first electrode, the second electrode, the third electrode and the fourth electrode are included in a second component block, and wherein the at least one first component block is connectable with the second component block.
 15. The medical device of claim 14, wherein the at least one first component block is connectable with the second component block via a plug and socket system.
 16. The medical device of claim 2, wherein the fourth electrode and the fifth electrode are arms of a forceps device.
 17. The medical device of claim 2, comprising: a filter to filter the smoke particles. 